Alzheimer Disease, Healthy
Conditions
Brief summary
A Phase 1, First-in-human, Randomized, Double-blind, Placebo-controlled, Single and Multiple Ascending Dose Study in Healthy Adults and Open-label Single Dose Study in Patients with Alzheimer's Disease to Assess the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of VG-3927.
Interventions
Dose Escalation
Dose Escalation
Sponsors
Study design
Eligibility
Inclusion criteria
* The participant is deemed healthy by the principal investigator, as determined by prestudy medical evaluation * The participant voluntarily agrees to participate in this study and signs an institutional review board approved informed consent
Exclusion criteria
* The participant has any concurrent disease or condition that, in the opinion of the principal investigator, would make the participant unsuitable for participation in the clinical study
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Adverse Events | 28 days post last dose | To evaluate the safety and tolerability of VG-3927 |
Countries
Australia, United States